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帕博西尼治疗方案在美国家庭肿瘤实践中的应用模式和临床结局。

Treatment patterns and clinical outcomes of palbociclib-based therapy received in US community oncology practices.

机构信息

Vector Oncology, an affiliate of ConcertAI, 6555 Quince, Suite 400, Memphis, TN 38119, USA.

Pfizer Inc., 235 East 42nd Street, NY 10017, USA.

出版信息

Future Oncol. 2021 Mar;17(9):1001-1011. doi: 10.2217/fon-2020-0744. Epub 2020 Nov 10.

Abstract

Limited studies have evaluated palbociclib-based therapy use in patients with advanced/metastatic breast cancer in the real world. This retrospective study used medical records from US community oncology practices to address the gap. Eligible patients receiving palbociclib-based therapy per label indication from 3 February 2015 to 31 December 2017 were included. Descriptive analyses were conducted for patient characteristics, treatment patterns and clinical outcomes. The study included 233 patients who received palbociclib + aromatase inhibitor (P+AI) and 48 who received palbociclib + fulvestrant (P+F). Real-world progression-free rate for P+AI was 69.8% (46.8%) at 12 (24) months (P+F: 43.5% [39.9%]) months. Real-world survival rate was 89.8% (71.4%) at 12 (24) months (P+F: 76.3% [65.0%]). The study findings are consistent with previous studies of palbociclib-based therapy.

摘要

有限的研究评估了帕博西尼为基础的治疗在真实世界中的晚期/转移性乳腺癌患者中的应用。这项回顾性研究使用了美国社区肿瘤学实践的病历来填补这一空白。符合条件的患者根据标签指示接受帕博西尼为基础的治疗,时间为 2015 年 2 月 3 日至 2017 年 12 月 31 日。对患者特征、治疗模式和临床结果进行了描述性分析。该研究包括 233 名接受帕博西尼+芳香酶抑制剂(P+AI)治疗的患者和 48 名接受帕博西尼+氟维司群(P+F)治疗的患者。P+AI 的真实无进展率为 12(24)个月时的 69.8%(46.8%)(P+F:43.5%[39.9%])。12(24)个月时的真实生存率为 89.8%(71.4%)(P+F:76.3%[65.0%])。研究结果与之前的帕博西尼为基础的治疗研究一致。

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